Evidence map›Paper›PMID 35166669›Full record

ArticleeLife2022

Intravital deep-tumor single-beam 3-photon, 4-photon, and harmonic microscopy.

Gert-Jan Bakker, Sarah Weischer, Júlia Ferrer Ortas, Judith Heidelin, Volker Andresen, Marcus Beutler, Emmanuel Beaurepaire, Peter Friedl

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
15.1field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  15. APL bioengineering · 2024
    Article
  16. Article
  17. Perfusion Window Chambers Enable Interventional Analyses of Tumor Microenvironments.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  18. Article
  19. Multidimensional Imaging of Breast Cancer.Cold Spring Harbor perspectives in medicine · 2023
    Review
  20. Metastasis from the tumor interior and necrotic core formation are regulated by breast cancer-derived angiopoietin-like 7.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 5 countries.

Gert-Jan BakkerDepartment of Cell Biology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Centre, Nijmegen, Netherlands.ORCID 0000-0003-3602-0014
Sarah WeischerDepartment of Cell Biology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Centre, Nijmegen, Netherlands.
Júlia Ferrer OrtasLaboratory for Optics & Biosciences École Polytechnique, CNRS, INSERM, Paris, France.
Judith HeidelinLaVision BioTec GmbH, a Miltenyi Biotec company, Bielefeld, Germany.
Volker AndresenLaVision BioTec GmbH, a Miltenyi Biotec company, Bielefeld, Germany.
Marcus BeutlerAPE Angewandte Physik & Elektronik GmbH, Berlin, Germany.
Emmanuel BeaurepaireLaboratory for Optics & Biosciences École Polytechnique, CNRS, INSERM, Paris, France.
Peter FriedlDepartment of Cell Biology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Centre, Nijmegen, Netherlands.ORCID 0000-0002-0119-4041
École Polytechnique · FRMiltenyi Biotec (Germany) · DERadboud University Nijmegen · NLAtlas Elektronik (United Kingdom) · GBThe University of Texas MD Anderson Cancer Center · US

Funding

European Research Council 617430
6 · The paper itself

Abstract

Three-photon excitation has recently been demonstrated as an effective method to perform intravital microscopy in deep, previously inaccessible regions of the mouse brain. The applicability of 3-photon excitation for deep imaging of other, more heterogeneous tissue types has been much less explored. In this work, we analyze the benefit of high-pulse-energy 1 MHz pulse-repetition-rate infrared excitation near 1300 and 1700 nm for in-depth imaging of tumorous and bone tissue. We show that this excitation regime provides a more than 2-fold increased imaging depth in tumor and bone tissue compared to the illumination conditions commonly used in 2-photon excitation, due to improved excitation confinement and reduced scattering. We also show that simultaneous 3- and 4-photon processes can be effectively induced with a single laser line, enabling the combined detection of blue to far-red fluorescence together with second and third harmonic generation without chromatic aberration, at excitation intensities compatible with live tissue imaging. Finally, we analyze photoperturbation thresholds in this excitation regime and derive setpoints for safe cell imaging. Together, these results indicate that infrared high-pulse-energy low-repetition-rate excitation opens novel perspectives for intravital deep-tissue microscopy of multiple parameters in strongly scattering tissues and organs.

Indexed as

Deep LearningAnimalsBone and BonesBrainCell Line, TumorCell SurvivalFluorescent DyesImage Processing, Computer-AssistedMaleMiceMicroscopy, Fluorescence, MultiphotonNeoplasms, ExperimentalSecond Harmonic Generation MicroscopyFluorescent Dyes3-photon microscopybonecancer biologycell biologyhumanmousenonlinear microscopythird harmonic generationtumor

Identifiers

PMID35166669
PMCPMC8849342
OpenAlexW4211183442

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.